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FGFR3 mutant dimers [plasma membrane]
Stable Identifier
R-HSA-2077412
Type
Set [DefinedSet]
Species
Homo sapiens
Compartment
plasma membrane
Locations in the PathwayBrowser
Expand all
Disease (Homo sapiens)
Diseases of signal transduction by growth factor receptors and second messengers (Homo sapiens)
Signaling by FGFR in disease (Homo sapiens)
Signaling by FGFR3 in disease (Homo sapiens)
Signaling by FGFR3 point mutants in cancer (Homo sapiens)
FGFR3 mutant receptor activation (Homo sapiens)
FGFR3 mutants bind and are inactivated by tyrosine kinase inhibitors (Homo sapiens)
FGFR3 mutant dimers [plasma membrane] (Homo sapiens)
FGFR3 mutant dimers:TKIs [plasma membrane] (Homo sapiens)
FGFR3 mutant dimers [plasma membrane] (Homo sapiens)
Participants
members
FGFR3c P250R mutant dimer bound to FGF [plasma membrane] (Homo sapiens)
FGFR3 (4;14) translocation mutant dimers [plasma membrane] (Homo sapiens)
FGFR3 point mutant dimers with enhanced kinase activity [plasma membrane] (Homo sapiens)
FGFR3 cysteine mutant dimers [plasma membrane] (Homo sapiens)
Participant Of
hasComponent
FGFR3 mutant dimers:TKIs [plasma membrane]
input
FGFR3 mutants bind and are inactivated by tyrosine kinase inhibitors
Disease
Name
Identifier
Synonyms
bone development disease
0080006
cancer
162
malignant tumor, malignant neoplasm, primary cancer
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